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The device is a noninvasive blood pressure measurement system intended to measure the systolic and diastolic blood pressures and pulse rate of an adult individual, over age 18, at home by using a non-invasive technique in which an inflatable cuff is wrapped around the wrist. The cuff circumference is limited to be 5.25" - 7.75".

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This document is a 510(k) clearance letter from the FDA for the Mytech/Happy Life Blood Pressure Monitor. It does not contain the acceptance criteria or a study proving the device meets those criteria.

Therefore, I cannot provide the requested information based on the provided text. The document confirms that the device is substantially equivalent to legally marketed predicate devices and can be marketed, but it does not detail the technical performance criteria or the studies conducted to establish that equivalence.

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